Understanding trunk control and muscle properties in acute stroke patients
Investigation of the Relationship Between Trunk Control and Viscoelastic Properties of Trunk Muscles in Acute Stroke Patients
NA · Sanko University · NCT06006988
This study is testing how trunk control and the stiffness of trunk muscles affect recovery in patients who have just had a stroke.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 30 (estimated) |
| Ages | 50 Years to 75 Years |
| Sex | All |
| Sponsor | Sanko University (other) |
| Locations | 1 site (Gaziantep) |
| Trial ID | NCT06006988 on ClinicalTrials.gov |
What this trial studies
This study investigates the relationship between trunk control and the viscoelastic properties of trunk muscles in patients who have experienced an acute stroke. It focuses on patients within the first 72 hours of an ischemic cerebrovascular event, assessing how changes in muscle stiffness and elasticity may impact recovery and functional outcomes. By utilizing the Myoton Pro device, the study aims to gather data on muscle characteristics that could inform targeted rehabilitation strategies. The findings could enhance our understanding of the early rehabilitation needs of stroke patients.
Who should consider this trial
Good fit: Ideal candidates include patients with ischemic stroke within the first 72 hours and a NIH score below 15, without additional neurological or orthopedic issues.
Not a fit: Patients who have had multiple strokes or those who are uncooperative may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved rehabilitation strategies that enhance trunk control and overall recovery in stroke patients.
How similar studies have performed: While there is existing research on trunk control in stroke patients, this specific focus on viscoelastic properties is relatively novel and has not been extensively tested.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patients with ischemic cerebro-vascular disease within the first 72 hours, * Patients with a National Institute of Health (NIH) score below 15 * No additional neurological and orthopedic problems * Patients who do not have any inconvenience in sitting hemodynamically * agree to participate in the study voluntarily Exclusion Criteria: * Patients who come to the service outside the first 72 hours * Uncooperative patients * patients who have had two or more strokes * Those who have had a Trans Ischemic Attack (TIA) * Refused to participate in the study
Where this trial is running
Gaziantep
- Sanko University — Gaziantep, Turkey (RECRUITING)
Study contacts
- Study coordinator: Hakan Polat
- Email: hakan.polat@sanko.edu.tr
- Phone: 05386487265
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Stroke